TY - JOUR
T1 - Modular development of a prototype point of care molecular diagnostic platform for sexually transmitted infections
AU - Branavan, Manoharanehru
AU - Mackay, Ruth E
AU - Craw, Pascal
AU - Naveenathayalan, Angel
AU - Ahern, Jeremy C
AU - Sivanesan, Tulasi
AU - Hudson, Chris
AU - Stead, Thomas
AU - Kremer, Jessica
AU - Garg, Neha
AU - Baker, Mark
AU - Sadiq, Syed T
AU - Balachandran, Wamadeva
N1 - Copyright © 2016 The Author(s). Published by Elsevier Ltd.. All rights reserved.
PY - 2016/4/22
Y1 - 2016/4/22
N2 - This paper presents the design of a modular point of care test platform that integrates a proprietary sample collection device directly with a microfluidic cartridge. Cell lysis, within the cartridge, is conducted using a chemical method and nucleic acid purification is done on an activated cellulose membrane. The microfluidic device incorporates passive mixing of the lysis-binding buffers and sample using a serpentine channel. Results have shown extraction efficiencies for this new membrane of 69% and 57% compared to the commercial Qiagen extraction method of 85% and 59.4% for 0.1ng/µL and 100ng/µL salmon sperm DNA respectively spiked in phosphate buffered solution. Extraction experiments using the serpentine passive mixer cartridges incorporating lysis and nucleic acid purification showed extraction efficiency around 80% of the commercial Qiagen kit. Isothermal amplification was conducted using thermophillic helicase dependant amplification and recombinase polymerase amplification. A low cost benchtop real-time isothermal amplification platform has been developed capable of running six amplifications simultaneously. Results show that the platform is capable of detecting 1.32×10(6) of sample DNA through thermophillic helicase dependant amplification and 1×10(5) copy numbers Chlamydia trachomatis genomic DNA within 10min through recombinase polymerase nucleic acid amplification tests.
AB - This paper presents the design of a modular point of care test platform that integrates a proprietary sample collection device directly with a microfluidic cartridge. Cell lysis, within the cartridge, is conducted using a chemical method and nucleic acid purification is done on an activated cellulose membrane. The microfluidic device incorporates passive mixing of the lysis-binding buffers and sample using a serpentine channel. Results have shown extraction efficiencies for this new membrane of 69% and 57% compared to the commercial Qiagen extraction method of 85% and 59.4% for 0.1ng/µL and 100ng/µL salmon sperm DNA respectively spiked in phosphate buffered solution. Extraction experiments using the serpentine passive mixer cartridges incorporating lysis and nucleic acid purification showed extraction efficiency around 80% of the commercial Qiagen kit. Isothermal amplification was conducted using thermophillic helicase dependant amplification and recombinase polymerase amplification. A low cost benchtop real-time isothermal amplification platform has been developed capable of running six amplifications simultaneously. Results show that the platform is capable of detecting 1.32×10(6) of sample DNA through thermophillic helicase dependant amplification and 1×10(5) copy numbers Chlamydia trachomatis genomic DNA within 10min through recombinase polymerase nucleic acid amplification tests.
KW - Animals
KW - DNA/genetics
KW - Hot Temperature
KW - Lab-On-A-Chip Devices
KW - Molecular Diagnostic Techniques/instrumentation
KW - Nucleic Acid Amplification Techniques
KW - Point-of-Care Systems
KW - Sexually Transmitted Diseases/diagnosis
U2 - 10.1016/j.medengphy.2016.04.022
DO - 10.1016/j.medengphy.2016.04.022
M3 - Article
C2 - 27238759
SN - 1350-4533
VL - 38
SP - 741
EP - 748
JO - Medical Engineering & Physics
JF - Medical Engineering & Physics
IS - 8
ER -